510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K001810Substantially Equivalent

Urisite Urine Collection Kit for Microalbumin/creatinine Testing

Flexsite Diagnostics, Inc., Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K001810 is the FDA 510(k) clearance record for URISITE URINE COLLECTION KIT FOR MICROALBUMIN/CREATININE TESTING, a class I device, cleared for Flexsite Diagnostics, Inc. on under FDA product code JIR (Indicator Method, Protein Or Albumin (Urinary, Non-Quant.)). FDA records list 2 510(k) clearances for Flexsite Diagnostics, Inc., from to . As of , FDA records show no recalls naming K001810.

Clearance record

Decision date
Received
(60 days to decision)
Product code
JIR Indicator Method, Protein Or Albumin (Urinary, Non-Quant.)
Regulation
21 CFR 862.1645
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Flexsite Diagnostics, Inc. 1900 K St. NW, Washington DC
510(k) summary
Summary
Third party review
No

Clearances, product code JIR

Trailing 12 months

FDA records hold no clearances under product code JIR in the trailing twelve months.

FDA records show no clearances under product code JIR in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code JIR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260